CZ292907B6 - Způsob převedení surového pigmentu do pigmentové formy - Google Patents

Způsob převedení surového pigmentu do pigmentové formy Download PDF

Info

Publication number: CZ292907B6
Authority: CZ; Czechia
Prior art keywords: pigment; acid; carboxylic acid; process according; salt
Prior art date: 1995-12-23

Application number

CZ19963807A

Other languages

Czech (cs)

English (en)

Other versions

CZ380796A3 (cs

Inventor

Paul Kerwin

Robert Langley

Arthur Stark Walls

Original Assignee

Ciba Specialty Chemicals Holding Inc.

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-12-23

Filing date

1996-12-20

Publication date

2004-01-14

1996-12-20 Application filed by Ciba Specialty Chemicals Holding Inc. filed Critical Ciba Specialty Chemicals Holding Inc.

1998-05-13 Publication of CZ380796A3 publication Critical patent/CZ380796A3/cs

2004-01-14 Publication of CZ292907B6 publication Critical patent/CZ292907B6/cs

Links

239000000049 pigment Substances 0.000 title claims abstract description 52
238000000034 method Methods 0.000 title claims abstract description 27
238000004898 kneading Methods 0.000 claims abstract description 18
150000003839 salts Chemical class 0.000 claims abstract description 16
239000007788 liquid Substances 0.000 claims abstract description 11
OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims description 15
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims description 15
150000001735 carboxylic acids Chemical class 0.000 claims description 9
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 5
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 4
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 4
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 4
239000005642 Oleic acid Substances 0.000 claims description 4
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
-1 amine salt Chemical class 0.000 claims description 4
MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 claims description 4
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 4
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 4
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 4
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
238000009835 boiling Methods 0.000 claims description 2
229940005605 valeric acid Drugs 0.000 claims description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims 1
230000000996 additive effect Effects 0.000 claims 1
PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 claims 1
RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 claims 1
150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 6
235000002639 sodium chloride Nutrition 0.000 description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
239000000203 mixture Substances 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 8
239000012065 filter cake Substances 0.000 description 8
239000002245 particle Substances 0.000 description 8
239000011780 sodium chloride Substances 0.000 description 8
239000003973 paint Substances 0.000 description 7
239000012452 mother liquor Substances 0.000 description 5
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
239000000725 suspension Substances 0.000 description 4
238000005406 washing Methods 0.000 description 4
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
239000001055 blue pigment Substances 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
230000005484 gravity Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
238000003801 milling Methods 0.000 description 2
239000001103 potassium chloride Substances 0.000 description 2
235000011164 potassium chloride Nutrition 0.000 description 2
239000002904 solvent Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
CGLVZFOCZLHKOH-UHFFFAOYSA-N 8,18-dichloro-5,15-diethyl-5,15-dihydrodiindolo(3,2-b:3',2'-m)triphenodioxazine Chemical compound CCN1C2=CC=CC=C2C2=C1C=C1OC3=C(Cl)C4=NC(C=C5C6=CC=CC=C6N(C5=C5)CC)=C5OC4=C(Cl)C3=NC1=C2 CGLVZFOCZLHKOH-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
239000004280 Sodium formate Substances 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
239000001639 calcium acetate Substances 0.000 description 1
235000011092 calcium acetate Nutrition 0.000 description 1
229960005147 calcium acetate Drugs 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
229960002713 calcium chloride Drugs 0.000 description 1
235000011148 calcium chloride Nutrition 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
239000012043 crude product Substances 0.000 description 1
150000005125 dioxazines Chemical class 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical class CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
150000002979 perylenes Chemical class 0.000 description 1
LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
229960001790 sodium citrate Drugs 0.000 description 1
235000011083 sodium citrates Nutrition 0.000 description 1
HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
235000019254 sodium formate Nutrition 0.000 description 1
239000001476 sodium potassium tartrate Substances 0.000 description 1
235000011006 sodium potassium tartrate Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000001256 steam distillation Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000002966 varnish Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0017—Influencing the physical properties by treatment with an acid, H2SO4

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Developing Agents For Electrophotography (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Paints Or Removers (AREA)
Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Coloring Foods And Improving Nutritive Qualities (AREA)
Saccharide Compounds (AREA)
Inorganic Compounds Of Heavy Metals (AREA)

CZ19963807A 1995-12-23 1996-12-20 Způsob převedení surového pigmentu do pigmentové formy CZ292907B6 (cs)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GBGB9526517.9A GB9526517D0 (en)	1995-12-23	1995-12-23	Production of pigments

Publications (2)

Publication Number	Publication Date
CZ380796A3 CZ380796A3 (cs)	1998-05-13
CZ292907B6 true CZ292907B6 (cs)	2004-01-14

Family

ID=10786070

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CZ19963807A CZ292907B6 (cs)	1995-12-23	1996-12-20	Způsob převedení surového pigmentu do pigmentové formy

Country Status (16)

Country	Link
US (1)	US5776238A (de)
EP (1)	EP0780446B1 (de)
JP (1)	JP3847395B2 (de)
KR (1)	KR100459619B1 (de)
CN (1)	CN1082983C (de)
AR (1)	AR005188A1 (de)
AT (1)	ATE203046T1 (de)
AU (1)	AU718788B2 (de)
BR (1)	BR9606128A (de)
CA (1)	CA2193605C (de)
CZ (1)	CZ292907B6 (de)
DE (1)	DE69613806T2 (de)
DK (1)	DK0780446T3 (de)
ES (1)	ES2160214T3 (de)
GB (1)	GB9526517D0 (de)
ZA (1)	ZA9610777B (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5105993A (en) *	1989-12-29	1992-04-21	La Haye Laboratories, Inc.	Disposable medical dispenser with a filtering dispenser nozzle
GB9808169D0 (en) *	1998-04-20	1998-06-17	Ciba Sc Holding Ag	Production process
US6013126A (en) *	1998-11-25	2000-01-11	Bayer Corporation	Process for conditioning organic pigments
JP4075286B2 (ja) *	1999-06-21	2008-04-16	東洋インキ製造株式会社	ハロゲンを含有しない緑色顔料組成物
MXPA01013296A (es) *	1999-07-09	2003-10-15	Ciba Sc Holding Ag	Pigmentos que tienen mejores propiedades coloristicas y procesos para su preparacion.
US6506244B1 (en)	1999-08-03	2003-01-14	Ciba Specialty Chemicals Corporation	Stable polymorphic copper-free phthalocyanine pigment
US20030177939A1 (en) *	2002-03-20	2003-09-25	Robertson George H.	Continuous process for preparing pigment flush
DE10257498A1 (de) *	2002-12-10	2004-07-01	Clariant Gmbh	Verfahren zur Herstellung von Phthalocyaninpigmentzubereitungen
WO2005078023A2 (de) †	2004-02-11	2005-08-25	Basf Aktiengesellschaft	Schwarze perylenpigmente
EP1807474A2 (de)	2004-11-01	2007-07-18	Ciba Specialty Chemicals Holding Inc.	Hochkonzentrierte fliessfähige pigmentmasse und verfahren zu ihrer herstellung
JP5124176B2 (ja)	2007-06-11	2013-01-23	三洋電機株式会社	ショーケース
ES2912282T3 (es) *	2013-07-31	2022-05-25	Dainippon Ink & Chemicals	Composición de pigmento de ftalocianina, método para la fabricación del mismo, y tinta
US20190334176A1 (en) *	2018-04-26	2019-10-31	Yeong Woo Kim	Devices and methods for preparing a slurry and coating a substrate with a slurry

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB710229A (en) *	1951-07-13	1954-06-09	Gen Aniline & Film Corp	Acid milling of vat dyestuffs
FR1156998A (fr) *	1956-07-26	1958-05-23	Gen Aniline & Film Corp	Empâtage acide de composés organiques de cuve
GB844405A (en) *	1956-08-14	1960-08-10	Ciba Ltd	Process for the production of vat dyestuff pigments in a finely divided form
US3510331A (en) *	1967-06-21	1970-05-05	Engelhard Min & Chem	Method for processing clay and product thereof
SE346576B (de) *	1967-12-05	1972-07-10	Ciba Geigy Ag
DE2336919C2 (de)	1973-07-20	1983-08-04	Bayer Ag, 5090 Leverkusen	Verfahren zur Formierung organischer Pigmente
US3963743A (en) *	1973-10-01	1976-06-15	Chemetron Corporation	Method of conditioning phthalocyanine pigments and product thereof
DE2738538A1 (de) *	1977-08-26	1979-03-01	Henkel Kgaa	Dispergieren von pigmenten
GB1589159A (en) *	1978-05-31	1981-05-07	Ciba Geigy Ag	Process for producing pigment and dyestuff compositions
DE2851752B1 (de) *	1978-11-30	1980-06-12	Basf Ag	Verfahren zur Herstellung von leichtdispergierbaren und farbstarken Pigmentformen
FR2446852A1 (fr) *	1979-01-19	1980-08-14	Ugine Kuhlmann	Compositions pigmentaires a base de phtalocyanines de cuivre et leur procede de fabrication
FR2508430B1 (de) *	1981-06-25	1985-12-13	Ici Francolor
EP0363322B1 (de) *	1988-10-06	1995-02-08	Ciba-Geigy Ag	Verfahren zur Herstellung von Pigmentzusammensetzungen
JP3132231B2 (ja) *	1993-04-23	2001-02-05	東洋インキ製造株式会社	顔料組成物および印刷インキもしくは塗料組成物
JP3344227B2 (ja) *	1996-07-29	2002-11-11	東洋インキ製造株式会社	微粒子イソインドリン系顔料及びその製造方法

1995
- 1995-12-23 GB GBGB9526517.9A patent/GB9526517D0/en active Pending
1996
- 1996-12-16 US US08/768,052 patent/US5776238A/en not_active Expired - Lifetime
- 1996-12-17 AU AU75428/96A patent/AU718788B2/en not_active Ceased
- 1996-12-17 AT AT96309202T patent/ATE203046T1/de not_active IP Right Cessation
- 1996-12-17 DK DK96309202T patent/DK0780446T3/da active
- 1996-12-17 DE DE69613806T patent/DE69613806T2/de not_active Expired - Lifetime
- 1996-12-17 EP EP96309202A patent/EP0780446B1/de not_active Expired - Lifetime
- 1996-12-17 ES ES96309202T patent/ES2160214T3/es not_active Expired - Lifetime
- 1996-12-20 CZ CZ19963807A patent/CZ292907B6/cs not_active IP Right Cessation
- 1996-12-20 BR BR9606128A patent/BR9606128A/pt not_active IP Right Cessation
- 1996-12-20 ZA ZA9610777A patent/ZA9610777B/xx unknown
- 1996-12-20 JP JP34030396A patent/JP3847395B2/ja not_active Expired - Fee Related
- 1996-12-20 AR ARP960105839A patent/AR005188A1/es unknown
- 1996-12-20 CA CA002193605A patent/CA2193605C/en not_active Expired - Fee Related
- 1996-12-21 CN CN96123902A patent/CN1082983C/zh not_active Expired - Fee Related
- 1996-12-21 KR KR1019960069913A patent/KR100459619B1/ko not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EP0780446A2 (de)	1997-06-25
JPH09194751A (ja)	1997-07-29
EP0780446B1 (de)	2001-07-11
MX9606748A (es)	1997-09-30
DE69613806T2 (de)	2001-12-06
CA2193605A1 (en)	1997-06-24
KR100459619B1 (ko)	2005-07-04
GB9526517D0 (en)	1996-02-28
ZA9610777B (en)	1997-06-23
US5776238A (en)	1998-07-07
DK0780446T3 (da)	2001-10-15
ATE203046T1 (de)	2001-07-15
AR005188A1 (es)	1999-04-14
AU718788B2 (en)	2000-04-20
CN1161358A (zh)	1997-10-08
CA2193605C (en)	2005-08-23
BR9606128A (pt)	1998-11-03
CN1082983C (zh)	2002-04-17
CZ380796A3 (cs)	1998-05-13
ES2160214T3 (es)	2001-11-01
DE69613806D1 (de)	2001-08-16
AU7542896A (en)	1997-06-26
KR970042859A (ko)	1997-07-26
EP0780446A3 (de)	1998-10-14
JP3847395B2 (ja)	2006-11-22

Legal Events

Date	Code	Title	Description
2000-06-30	PD00	Pending as of 2000-06-30 in czech republic
2008-08-06	MM4A	Patent lapsed due to non-payment of fee	Effective date: 20071220

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